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NCT07325136 · ClinicalTrials.gov registry record · Phase 1

A Study to Assess the Safety and Tolerability of BMS-986525 Alone and in Combination With Nivolumab in Participants With Relapsed/Refractory Small Cell Lung Cancer

A Phase 1 study of Relapsed/Refractory Small Cell Lung Cancer, sponsored by Bristol-Myers Squibb.

Recruiting
Registry status
Phase 1
Development phase
240
Enrollment target
11
Study locations

NCT07325136 is a Phase 1 study of Relapsed/Refractory Small Cell Lung Cancer that is actively recruiting participants, run by Bristol-Myers Squibb. The registered enrollment target is 240 participants. The trial reports 11 study locations across 10 states.

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The verdict

NCT07325136, a Phase 1 study of Relapsed/Refractory Small Cell Lung Cancer, is actively recruiting participants, sponsored by Bristol-Myers Squibb.

RECRUITING
Registry status
Phase 1
Development phase
240 participants
Enrollment target
11
Study locations

Study Summary

The purpose of this study is to assess the safety and tolerability of BMS-986525 alone and in combination with Nivolumab in participants with Relapsed/Refractory Small Cell Lung Cancer

Interventions

  • DRUG Nivolumab
  • DRUG BMS-986525

Study Locations (11)

Other

  • Local Institution - 0003 - Craiova
  • Local Institution - 0009 - Madrid

Michigan

  • Local Institution - 0011 - Detroit

New York

  • Local Institution - 0026 - Buffalo

North Carolina

  • Local Institution - 0005 - Durham

Ohio

  • University Hospitals Cleveland Medical Center - Cleveland

Tennessee

  • SCRI Oncology Partners - Nashville

Milano

  • Local Institution - 0001 - Rozzano

Osaka

  • Local Institution - 0020 - Hirakata

Trial Details

FieldValue
Enrollment Target 240 participants
Start Date 2026-02-03
Est. Completion 2029-04-24
Phase Phase 1

Sponsor

Bristol-Myers Squibb

1,025 total trials

What the Registry Record Tells You About NCT07325136

The ClinicalTrials.gov registry entry for NCT07325136 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 240 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bristol-Myers Squibb, which has 1,025 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Relapsed/Refractory Small Cell Lung Cancer appearing as the primary indexed condition, and to 2 interventions - of which Nivolumab is the first listed.

NCT07325136 reports 11 study locations spanning 10 distinct geographic areas - top geographies include Other, Michigan, New York.

Frequently Asked Questions

What is clinical trial NCT07325136 about?

NCT07325136 is a clinical study titled "A Study to Assess the Safety and Tolerability of BMS-986525 Alone and in Combination With Nivolumab in Participants With Relapsed/Refractory Small Cell Lung Cancer". The purpose of this study is to assess the safety and tolerability of BMS-986525 alone and in combination with Nivolumab in participants with Relapsed/Refractory Small Cell Lung Cancer

What is the current status of trial NCT07325136?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 240 participants. The study started on 2026-02-03. Estimated completion is 2029-04-24.

What conditions does trial NCT07325136 study?

This clinical trial studies the following conditions: Relapsed/Refractory Small Cell Lung Cancer.

What interventions are being tested in trial NCT07325136?

The interventions under investigation include: Nivolumab (DRUG), BMS-986525 (DRUG).

Who is sponsoring clinical trial NCT07325136?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07325136 being conducted?

This trial has 11 study locations across Michigan, New York, North Carolina, Ohio, Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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